Comprehensive characterization by UHPLC-ESI-Q-TOF-MS from an Eryngium bourgatii extract and their antioxidant and anti-inflammatory activities

被引:118
作者
de la Luz Cadiz-Gurrea, Maria [1 ,2 ]
Fernandez-Arroyo, Salvador [1 ,2 ]
Joven, Jorge [3 ]
Segura-Carretero, Antonio [1 ,2 ]
机构
[1] Univ Granada, Fac Sci, Dept Analyt Chem, E-18071 Granada, Spain
[2] Funct Food Res & Dev Ctr, Armilla 18100, Granada, Spain
[3] Univ Rovira & Virgili, IISPV, Hosp Univ St Joan, Ctr Recerca Biomed, E-43201 Reus, Tarragona, Spain
关键词
Eryngium bourgatii; UHPLC-ESI-Q-TOF-MS; Phenolic compounds; Antioxidant activity; Anti-inflammatory properties; CHLOROGENIC ACID; CAPACITY; GLYCOSIDES;
D O I
10.1016/j.foodres.2012.09.038
中图分类号
TS2 [食品工业];
学科分类号
100403 [营养与食品卫生学];
摘要
The genus Eryngium (family Apiaceae) consists of about 300 species. This genus is known to contain polyacetylenes, flavonoids and saponins, coumarins, and monoterpene glycosides. In folk medicine, various species are used for a wide range of foods; particularly roots are used against various inflammatory disorders, oedema, sinusitis, urinary infections, etc. The aim of the present study was to characterize phenolic compounds in the leaves and flowers of Eryngium bourgatii using UHPLC-ESI-Q-TOF-MS. A total of 44 compounds were identified belonging to various structural classes such as flavonols (quercetin, kaempferol, isorhamnetin and derivatives), flavanones (naringenin rhamnoglucoside), cinnamic acids (chlorogenic, rosmarinic, ferulic and caffeic acids and derivatives), benzoic acids (p-hydroxybenzoic acid glucoside, arbutin, syringic acid, glucogallin, and gentisic acid and derivatives) and other organic acids (gluconic, citric, and quinic acids and derivatives). The method described simultaneously a wide range of phenolic compounds and a tentative characterization was made of the major compounds of this extract. In addition, E. bourgatii extract shows antioxidant activity (by TEAC, FRAP and ORAC methods) and anti-inflammatory properties, decreasing the generation of reactive oxygen species and inhibiting the production of MCP-1 and their transcripts, respectively, in TNF-alpha-induced HUVEC. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:197 / 204
页数:8
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